INNO-LIA HCV Score. KEY-CODE: INX INNO-LIA HCV Score v p 1/12. English

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1 p 1/12 INNO-LIA HCV Score Manufactured by: INNOGENETICS N.V. Technologiepark Gent Belgium BTW BE RPR Gent Distributed by: INNOGENETICS GmbH Hans-Böckler-Allee Hannover Germany INNOGENETICS S.r.l. Via Vaccareccia 39/A Pomezia (Roma) Italy INNOGENETICS s.a.r.l. Les Conquérants, Bât. Le Kilimandjaro 8/10, avenue des Tropiques Les Ulis France INNOGENETICS Diagnóstica Iberia, S.L.U. Calle Tarragona 161, Planta Barcelona Spain "Note changes highlighted INNOGENETICS N.V. Technologiepark Gent Belgium Other languages see / Autres langues voir / Andere Sprachen siehe / Altre lingue vedere / Ver otros idiomas / Outras línguas ver: EUROPE GR IS LT RO SK LI MT 8:00 17:00 GMT+1 M T W T F S S 2010 Innogenetics

2 p 2/12 TABLE OF CONTENTS Symbols used...3 Intended use...4 Test principle...4 Reagents...4 Description, preparation for use and recommended storage conditions...4 Materials required but not provided...5 Safety and environment...5 Specimen (collection and handling)...5 Remarks and precautions...6 Manual test procedure...6 Directions for washing...7 Directions for incubation...7 Automated test procedure: Auto-LIA...8 Results...9 Reading...9 Validation...10 Interpretation of the results...10 Interpretation software: LiRAS for Infectious diseases...10 Limitations of the procedure...10 Test performance...11 Sensitivity...11 Specificity...12 Reproducibility...12 Trademarks...12

3 p 3/12 Symbols used Manufacturer In Vitro Diagnostic Medical Device Batch code Catalogue number Use By Consult Instructions for Use Temperature limitation Biological risks Contains sufficient for <n> tests Conjugate Negative Control Positive Control Sample Diluent Stop Solution Strips Substrate BCIP/NBT Wash Solution 5x

4 p 4/12 Intended use The INNO-LIA HCV Score is a Line Immuno Assay (LIA ) for the detection of antibodies to human hepatitis C virus in human serum or plasma. It is intended for use as a supplementary test on human serum or plasma specimens found to be reactive using an anti-hcv screening procedure. Test principle The INNO-LIA HCV Score is a 3 rd generation line immunoassay which incorporates HCV antigens derived from the core region, the E2 hypervariable region (HVR), the NS3 helicase region, the NS4A, NS4B, and NS5A regions. The antigens were coated as 6 discrete lines on a nylon strip with plastic backing. In addition, four control lines are coated on each strip: streptavidin control line, 3+ positive control (anti-human Ig) which is also used as sample addition control line, 1+ positive control (human IgG), and the ± cut-off line (human IgG). The INNO-LIA HCV Score is based on the principle of an enzyme immunoassay. A test sample is incubated in a trough together with the test strip. If present in the sample, HCV antibodies will bind to the HCV antigen lines on the strip. Subsequently, an affinity-purified alkaline phosphatase-labelled goat anti-human IgG (H+L) conjugate is added and reacts with specific HCV antigen/antibody complexes, if previously formed. Incubation with the enzyme substrate produces a chesnut-like color, the intensity of which is proportionate to the amount of HCV-specific antibody captured from the sample on any given line (Fig.1). Color development is stopped with sulfuric acid. Reagents Description, preparation for use and recommended storage conditions - If kept at 2-8 C, opened or unopened, all reagents are stable until the expiration date. Do not freeze reagents. Do not use the kit beyond the expiration date. - All reagents and the plastic tube containing the test strips must be brought to room temperature (18-25 C) approximately 30 minutes before use and returned to the refrigerator (2-8 C) immediately after use. - Alterations in the physical appearance of kit reagents may indicate instability or deterioration. - After opening the original tube containing the strips, any unused strip will be stable for 16 weeks if stored at 2-8 C in the closed original tube with desiccant. Reagents supplied: Component Quantity Ref. Description Strips Containing 20 INNO-LIA HCV antigen-coated test strips. Sample Diluent 30 ml Containing color-coded (green) phosphate buffer containing sodium chloride, detergent, bovine protein stabilizers and 0.3% chloroacetamide (CAA) as preservative. Ready-to-use Conjugate 45 ml Containing color-coded (red) goat anti-human IgG labeled with alkaline phosphatase in Tris buffer containing bovine stabilizers, detergent and 0.01% methylisothiazolone (MIT)/0.1% CAA as preservative. Negative Control 0.12 ml Containing basematrix of human origin with 0.01% MIT/0.1% CAA as preservative. Positive Control 0.12 ml Containing inactivated human serum positive for antibodies to HCV with 0.01% MIT/0.1% CAA as preservative. Ready-to-use BCIP/NBT Substrate 45 ml Containing 5-bromo-4-chloro-3-indolyl phosphate/nitroblue tetrazolium in dimethyl formamide, with 0.01% MIT/0.1% CAA as preservative. Stop Solution 45 ml Containing 0.1 mol/l sulfuric acid. Wash Solution 45 ml Containing color-coded (blue) Tris buffer containing sodium chloride, detergent and 0.02% bromo-nitro-dioxane as preservative, to be diluted 5x in distilled water. Diluted wash solution is stable for 2 weeks if kept at 2-8 C. Incubation tray 2 - With 11 troughs each. Adhesive sealers 5 - Data reporting sheet 1 - For storage of developed strips. Reading card 1 - For identification of reactive antigen lines.

5 p 5/12 Materials required but not provided - Distilled or deionized water. - Precision pipettes (with disposable tip) capable of delivering 10 µl, µl, and µl, respectively. - Orbital shaker or rocker (see Directions for incubation). - Vortex mixer or equivalent. - Graduated cylinders: 10, 25, 50, and 100 ml. - Tweezers for strip handling. - Timer. - Optional: hot air fan (hair dryer) or dry incubator at 37 C. a repetitive pipette together with disposable vials for the addition of stop solution, conjugate, substrate and wash solution. vacuum aspirator which contains 5% sodium hypochlorite solution in a waste bottle. Safety and environment Please refer to the Material Safety Data Sheet (MSDS) and product labelling for information on potentially hazardous components. The most recent MSDS version is available on the website Irritant! (Xi) R43, S Contains 2-Chloroacetamide: CONJ, SUBS BCIP/NBT, CONTROL -, SAMP DIL R43 May cause sensitization by skin contact. S23 Do not breathe vapour/spray. S24 Avoid contact with skin. S37 Wear suitable gloves. S60 This material and its container must be disposed of as hazardous waste. - Specimens, Positive Control and Negative Control should always be handled as potentially infectious. - The Positive Control has been found to be negative for anti-hiv and HbsAg. The Negative Control has been found to be negative for anti-hiv-1/hiv-2, anti-hcv and HbsAg. No test method can offer complete insurance that blood products will not transmit infectious agents. Therefore, all blood components and biological materials should be considered as being potentially infectious and should be handled as such. Only adequately trained personnel should be permitted to perform the test procedure. All blood components and biological materials should be disposed of in accordance with established safety procedures. Autoclave for at least 15 minutes at 121 C. Incinerate disposable material. Mix liquid waste with sodium hypochlorite so that the final concentration is ± 1% sodium hypochlorite. Allow to stand overnight before disposal. CAUTION: Neutralize liquid waste that contains acid before adding sodium hypochlorite. - Use of personal protective equipment is necessary: gloves and safety spectacles when manipulating dangerous or infectious agents. - Waste should be handled according to the institution's waste disposal guidelines. All federal, state, and local environmental regulations should also be observed. - Do not aspirate the stop solution in a waste bottle, which contains sodium hypochlorite. Specimen (collection and handling) - The INNO-LIA HCV Score may be performed on human serum or plasma collected in tubes containing citrate, heparin or EDTA as anticoagulants. - Before storage, serum or plasma should be separated from blood clot or blood cells by centrifugation. - Store the specimens at 2-8 C. For storage longer than one week, freeze at -20 C or lower. - Do not use heat-treated specimens. - Repeatedly (more than 3 times) frozen and thawed samples may produce erroneous results.

6 p 6/12 Remarks and precautions - Do not mix reagents with different lot numbers. - Frozen reagents, eg. stored too close to cooling element, can cause erroneous results! - Make sure correct sample volume and washing times are used for the test procedure needed. - Avoid microbial contamination of reagents. - Ensure that the samples and controls are homogeneous before use. - Do not touch the membrane of the strip. Always manipulate the strips with the plastic backing. - Use a new pipette tip for each specimen. - Make sure that the test strips are placed in the troughs with their membrane side facing upwards. - All incubation steps should be performed using an orbital shaker or rocker (use rocker only for overnight sample incubation). The shaking of the solutions over the strips is important in achieving even line staining and maximum sensitivity. During shaking, the strip surface should be completely submerged. - Cover the throughs with an adhesive sealer to avoid drying of the strips during the overnight sample incubation. - Unused and developed strips should be kept away from strong light and heat. - The kit should only be used by personnel trained in clinical laboratory practices. - Re-use of strips or troughs will result in erroneous results. - Cutting strips will result in erroneous interpretation of the results. Manual test procedure Please read Remarks and precautions before performing the test hours sample incubation 1. Use the required amount of test troughs, taking into account that for each test run, a Positive and a Negative Control should be assayed. Identify test troughs as controls and specimens, and place them in the tray. 2. Add 1 ml of Sample Diluent to each test trough. 3. Add 10 µl of the appropriate specimen or control to the appropriately labelled trough. 4. Remove the required amount of test strips from their container, and add one strip to each of the test troughs. The test strip is placed membrane side upwards into the trough using tweezers. THE STRIP MUST BE COMPLETELY SUBMERGED. 5. Cover the troughs with an adhesive sealer (see Remarks and precautions). Incubate the samples by placing the tray on a shaker or rocker (see Direction for incubation) and agitate OVERNIGHT (16 ± 2 h) at room temperature (18-25 C). NOTE: Carefully remove the adhesive sealers to avoid cross-contamination. 6. Wash each test strip 3 times (5 minutes) with 1 ml Wash Solution (see Directions for washing). 7. Add 1 ml of Conjugate Solution to each test trough. 8. Incubate with the conjugate by placing the test tray on the shaker or rocker and agitate for 30 minutes at room temperature (18-25 C). 9. Wash each test strip 3 times (5 minutes) with 1 ml Wash Solution (See Directions for washing). 10. Add 1 ml of Substrate Solution to each test trough. 11. Incubate with the substrate by placing the test tray on the shaker or rocker, and agitate for 30 minutes at room temperature (18-25 C). 12. Aspirate liquid. Add 1 ml of Stop Solution to each trough. 13. Incubate with the stop solution by placing the test trough on the shaker or rocker, and agitate for minutes at room temperature (18-25 C). 14. Aspirate Stop Solution. 15. Remove the strips from the test troughs and place them, membrane side upwards, on absorbent paper using tweezers. As soon as the strips have dried completely, results can be interpreted. To accelerate the drying process, place strips in a dry incubator at 37 C for 30 minutes or use a hot air fan for 1 minute. Developed strips will retain their color if stored in the dark. - 2 and 3 hours sample incubation For the "2 hours and 3 hours sample incubation" protocol the same 15 steps as for the test procedure "16 hours sample incubation" will be followed, but changes to steps and 9 have to be taken into account. Sample volume for specimens and controls will increase from 10 to 20 µl (step 3) and sample incubation time changes to 2 and 3 hours (step 5). Washing after sample incubation changes for the 2 hours procedure to 3

7 p 7/12 times 10 minutes and for the 3 hours procedure to 3 times 6 minutes (step 6); finally the second washing is 3 times 3 minutes for the 2 and 3 hours sample incubation (step 9). Summary test procedures with highlighted differences (bold), given in following table: 16 hours sample incubation 2 hours sample incubation 3 hours sample incubation Sample Diluent 1 ml 1 ml 1 ml Specimen 10 µl 20 µl 20 µl Controls 10 µl 20 µl 20 µl LIA test strips 16 hours ± 2 hours 2 hours 3 hours Washing 1 ml/3 x 5 min 1 ml/3 x 10 min 1 ml/3 x 6 min RTU* Conjugate 1 ml/30 min 1 ml/30 min 1 ml/30 min Washing 1 ml/3 x 5 min 1 ml/3 x 3 min 1 ml/3 x 3 min RTU* Substrate 1 ml/30 min 1 ml/30 min 1 ml/30 min Stop Solution 1 ml/10-30 min 1 ml/10-30 min 1 ml/10-30 min *RTU = Ready-to-use Directions for washing - After overnight, 2 hours and 3 hours incubation, carefully remove the adhesive plate sealer. - The liquid is aspirated from the trough with a pipette, preferentially attached to a vacuum aspirator, which contains 5% sodium hypochlorite solution in the waste bottle. The tray is held at an angle to allow all liquid to flow to one side of the trough (to the uncoated plastic backing part of each strip). - Add 1 ml of diluted wash solution to each trough and agitate on a shaker or rocker. Shaking time is indicated in the assay procedure. - Repeat these steps as many times as indicated in the assay procedure. NOTE: Do not allow the strips to dry between the washing steps. Make sure not to damage the surface of the test strips when aspirating. Always use a clean aspiration device with disinfectant trap to avoid cross-contamination. Make sure the entire strip is thoroughly washed by complete submersion in the washing solution. Adapt the speed of the shaker or rocker when necessary. Avoid splashing of the Wash Solution over the edges of the troughs. Directions for incubation - All the incubation steps (sample, conjugate, substrate, and stop solution incubation) and also the washing steps should be performed on a shaker or rocker (use rocker only for overnight sample incubation). - During incubation and washing steps, the strip surface should be completely submerged, with the membrane side facing upwards. - The shaker or rocker should allow a reciprocal (to- and- fro) motion of the strips in the trough, and a movement of the liquid over the strips without spilling over the trough. - The speed generated by an orbital or longitudinal shaker or rocker is critical in achieving even line staining and maximum sensitivity. Recommendations for an orbital shaker: diameter of the circular motion should be equal or superior to 13 mm recommended speed for a 13 mm circular motion is 160 rpm recommended speed for a 24 mm circular motion is 90 rpm. Recommendations for a rocker: the difference between highest and lowest point should not exceed 80 mm to avoid spilling of liquid recommended speed is 34 rpm.

8 p 8/12 Automated test procedure: Auto-LIA The LIA test procedure can easily be automated using the Auto-LIA automate. This instrument is a walk-away system with automated aspiration, pipetting, and incubation. For more information on the Auto-LIA, please contact Innogenetics or your local distributor. Please read Remarks and precautions before performing the test. Detailed Auto-LIA procedures - 16 hours sample incubation Auto-LIA 1. DISP CH1 Stpos: Begin Endpos: Till end 1000 µl 2. INC 1 min, shake speed 4 3. PAUSE 4. INC 960 min, shake speed 4 5. WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 6. INC 6 min, shake speed 4 7. WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 8. INC 6 min, shake speed 4 9. WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 10. INC 6 min, shake speed ASP 12. DISP CH4 Stpos: Begin Endpos: Till end 1000 µl 13. INC 30 min, shake speed WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 15. INC 3 min, shake speed WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 17. INC 3 min, shake speed WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 19. INC 3 min, shake speed ASP 21. DISP CH6 Stpos: Begin Endpos: Till end 1000 µl 22. INC 30 min; shake speed ASP 24. DISP CH5 Stpos: Begin Endpos: Till end 1000 µl 25. INC 20 min, shake speed ASP 27. END - 2 hours sample incubation Auto-LIA 1. DISP CH1 Stpos: Begin Endpos: Till end 1000 µl 2. INC 1 min, shake speed 4 3. PAUSE 4. INC 120 min, shake speed 4 5. WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 6. INC 10 min, shake speed 4 7. WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 8. INC 10 min, shake speed 4 9. WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 10. INC 10 min, shake speed ASP 12. DISP CH4 Stpos: Begin Endpos: Till end 1000 µl 13. INC 30 min, shake speed WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 15. INC 3 min, shake speed WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 17. INC 3 min, shake speed WASH CH2 Stpos: Begin Endpos: Till end 1000 µl 19. INC 3 min, shake speed ASP 21. DISP CH6 Stpos: Begin Endpos: Till end 1000 µl

9 p 9/ INC 30 min; shake speed ASP 24. DISP CH5 Stpos: Begin Endpos: Till end 1000 µl 25. INC 20 min, shake speed ASP 27. END CH1 = Sample Diluent CH2 = Wash Solution CH4 = Conjugate CH5 = Stop Solution CH6 = Substrate - 3 hours sample incubation Auto-LIA For the "3 hours sample incubation" protocol the same 27 steps as for the test procedure "2 hours sample incubation" will be followed, but changes to steps and 10 have to be taken into account. Sample incubation time changes to 180 minutes for the 3 hours procedure (step 4) and washing after 3 hours sample incubation changes to 3 times 6 minutes (steps ). Results Reading The identity and location of the antigens and controls coated on the strip are as follows: Figure 1: INNO-LIA HCV Score test strip The intensity of the reaction on the control lines on each strip is used to assign the reactivity ratings for each antigen on that strip: Intensity of antigen line reaction (R) Rating Lower than ± R < ± - Equal to ± R = ± ± Higher than ±, but lower or equal to 1+ ± < R Higher than 1+ but lower than < R < Equal to 3+ R = Higher than 3+ R > A reactivity rating must be made separately for each strip. Use the reading card for correct interpretation. Identification of the lines is obtained by alignment of the 3+ control line on the developed strip with the corresponding 3+ control line on the reading card.

10 p 10/12 Validation Check the validity of the positive and the negative control strips and the validity of the control levels on each strip before reading the test results. Validation of the test run: 1. The positive control strip must show a reaction of at least 1+ on C1, C2, NS3 and NS4 antigen line. The E2 and NS5 antigen line may show a negative rating. 2. The negative control strip must show a negative rating (no reaction at all or at least less than control level ± for all the HCV antigen lines). Validation of a single strip: 1. The control levels 1+ and ± as well as the strong positive control level 3+ should be visible. 2. The intensity of the control level 3+ should be greater than that of level 1+ and the intensity of the level 1+ should be greater than that of level ±. 3. The control line for anti-streptavidin should have a negative rating. NOTE: The strip must be completely dried to avoid any misinterpretation due to faintly visible bands appearing after addition of stop solution. Do not place paper on top of the strips as long as they are wet. Weak control bands can be observed for samples containing high IgG levels (above the normal IgG range). Interpretation of the results Extensive evaluations have shown that results may be interpreted as follows: A sample is NEGATIVE for HCV antibodies: - if all HCV antigen lines have a negative reactivity rating - if only one HCV antigen line has a reactivity of ±, except when the reactivity is observed for NS3. A sample is POSITIVE for HCV antibodies: - if at least two HCV antigen lines have a reactivity of ± minimum or higher. A sample is considered INDETERMINATE for HCV antibodies: - if one HCV antigen line has a reactivity rating of 1+ or higher - if the NS3 line reacts with a reactivity of ± or higher and all other antigen lines are negative. Interpretation software: LiRAS for Infectious diseases The LiRAS for infectious diseases software is designed to assist with the interpretation of the LIA results. Please contact your local distributor to obtain the latest updated version. WARNING: Do not use the automated interpretation without taking into account the limitations of the procedure mentioned below. Limitations of the procedure - The protocol provided must be strictly followed to obtain optimal performance of the assay. - Samples with a single +/- reactivity or higher on NS3 can be indicative for HCV seroconversion. They are therefore scored as indeterminate. - If an INDETERMINATE result is obtained, it is recommended to test an additional patient sample after a few weeks. - A sample giving a positive reaction on the streptavidin control line may give cross-reactions with other HCV antigens lines and can not be determined as positive for HCV antibodies. - Anti-HCV antibodies may be undetectable in early infection. - In a hemodialysis setting antibodies may be undetectable. - The use of diluted samples may give erroneous results. - Parameters for assessing liver damage and HCV RNA positivity should be further investigated in HCV antibodypositive subjects before initiating treatment or invasive procedures.

11 p 11/12 Test performance Sensitivity Seroconversion panels/low-titer panels The results of the INNO-LIA HCV Score using the Auto-LIA 2-hour sample incubation procedure and the manual 16-hour sample incubation procedure were obtained internally on 13 BBI seroconversion panels (PHV 904 till 916), on 2 BBI low titer panels (PHV103 and 204), and on the SFTS94 panel. The 13 seroconversion panels started with a negative bleed and had narrow bleeding intervals. These results were compared with CHIRON RIBA HCV 3.0 SIA results (Table 1 and Table 2). Table 1: Overview results BBI seroconversion panels Detection seroconversion panels towards Chiron RIBA HCV 3.0 SIA Assay Earlier Equal Later Stayed negative INNO-LIA HCV Score (2 hours Auto-LIA procedure) INNO-LIA HCV Score (16 hours manual procedure) Table 2: Overview results BBI low titer panels and SFTS94 panel Number of detected positive samples/panel Assay PHV 103 PHV 204 SFTS 94 INNO-LIA HCV Score (2 hours Auto-LIA procedure) INNO-LIA HCV Score (16 hours manual procedure) CHIRON RIBA HCV 3.0 SIA HCV-positive samples A total of 257 samples, originating from HCV-infected patients and found to be positive on 2 screening assays, were analyzed internally on the INNO-LIA HCV Score using the Auto-LIA 2-hour sample incubation procedure. All samples scored positive, with the exception of a single sample which scored indeterminate. In addition, the INNO-LIA HCV Score using the Auto-LIA 2-hour sample incubation procedure was performed internally on 99 HCV genotyped samples. All major HCV genotypes were covered in the sample set (Table 3). Table 3. Genotype distribution of the tested HCV- positive samples Genotype of tested samples No. samples tested a 15 1b a a 15 4 non-a Total 99 Note: no genotype 6 sample was available for testing. All 99 positive samples scored positive. In total, this is resulting in a sensitivity, upon inclusion of the single indeterminate result, of 100% (356/356; 95% CI [98,9%; 100,0%]).

12 p 12/12 Specificity Blood donors A total of 400 blood donors found to be negative for HCV antibodies were analyzed internally using the manual 16-hour sample incubation procedure. After initial testing, 377 samples were scored negative, 22 samples scored indeterminate, and one sample scored positive, resulting in an initial specificity of 94.3% (377/400; 95% CI [91.5%; 96.1%]). The initial positive blood sample scored negative after repeated testing in duplicate, resulting in a specificity after re-testing of 94.5% (378/400; 95% CI [91.8%; 96.3%]). Clinical samples Two hundred five clinical samples were tested internally using the manual 16-hour sample incubation procedure. One hundred eighty-nine of them scored negative, 11 were indeterminate, and 5 scored positive. Three of these 5 samples scored negative after repeated testing in duplicate. One of the other 2 samples scored positive after repeated testing, while the other sample scored indeterminate. Both samples were negative on Ortho HCV 3.0 ELISA with Enhanced SAVe and on INNOTEST HCV Ab IV. One of these 2 samples was tested on CHIRON RIBA HCV 3.0 SIA as well, and was found to be negative. For this sample set, an initial specificity of 92.2% (189/205; 95% CI [87.7%; 95.1%]) was obtained, while specificity after repeated testing was 93.7% (192/205; 95% CI [89.5%; 96.3%]). Potentially interfering samples One hundred thirty-seven potentially interfering samples were tested internally using the manual 16-hour sample incubation procedure. One hundred twenty-seven samples turned out to be negative, 9 were indeterminate, and one scored positive. Upon repeated testing in duplicate, this sample scored positive, and indeterminate, respectively. This sample was found to be negative on Ortho HCV 3.0 ELISA with Enhanced SAVe, on INNOTEST HCV Ab IV, and on CHIRON RIBA HCV 3.0 SIA. On this set of samples, a specificity of 92.7% (127/137; 95% CI [87.1%; 96.0%]) was obtained. Reproducibility Two experimenters tested a panel of 13 HCV-positive samples, as well as one positive and one negative control on 3 different lots using the Auto-LIA 2-hour sample incubation procedure while a third experimenter tested this panel on one of these lots. The use of different strip lots and performance by different experimenters resulted in the same test outcome. Trademarks - INNOGENETICS and LIA are Registered Trademarks of Innogenetics N.V. - INNO-LIA is a Trademark of Innogenetics N.V.